EC Number   |
BRENDA No. |
Title |
Journal |
Volume |
Pages |
Year |
Organism |
PubMed ID |
|---|
   2.4.1.313 | 759014 |
Detecting and imaging O-GlcNAc sites using glycosyltransferases a systematic approach to study O-GlcNAc |
Cell Chem. Biol. |
25 |
1428-1435 |
2018 |
Homo sapiens |
30100348 |
| 2.4.1.313 | 759500 |
Identification of mammalian glycoproteins with type-I LacdiNAc structures synthesized by the glycosyltransferase B3GALNT2 |
J. Biol. Chem. |
294 |
7433-7444 |
2019 |
Cricetulus griseus |
30898876 |
| 2.4.1.313 | 759500 |
Identification of mammalian glycoproteins with type-I LacdiNAc structures synthesized by the glycosyltransferase B3GALNT2 |
J. Biol. Chem. |
294 |
7433-7444 |
2019 |
Homo sapiens |
30898876 |
| 2.4.1.313 | 725358 |
A novel human beta1,3-N-acetylgalactosaminyltransferase that synthesizes a unique carbohydrate structure, GalNAcbeta1-3GlcNAc |
J. Biol. Chem. |
279 |
14087-14095 |
2004 |
Homo sapiens |
14724282 |
| 2.4.1.313 | 736048 |
B3GALNT2 is a gene associated with congenital muscular dystrophy with brain malformations |
Eur. J. Hum. Genet. |
22 |
707-710 |
2014 |
Homo sapiens |
24084573 |
| 2.4.1.313 | 725164 |
Involvement of B3GALNT2 overexpression in the cell growth of breast cancer |
Int. J. Oncol. |
44 |
427-434 |
2014 |
Homo sapiens |
24285400 |
| 2.4.1.313 | 723906 |
Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of alpha-dystroglycan |
Am. J. Hum. Genet. |
92 |
354-365 |
2013 |
Danio rerio |
23453667 |
| 2.4.1.313 | 723906 |
Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of alpha-dystroglycan |
Am. J. Hum. Genet. |
92 |
354-365 |
2013 |
Homo sapiens |
23453667 |
| 2.4.1.313 | 726488 |
SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function |
Science |
341 |
896-899 |
2013 |
Homo sapiens |
23929950 |
